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Items: 1 to 20 of 185

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5979182inversion1nstd209human GRCh38 chr7: 99,981,419-101,289,122 , GRCh37.p13 chr7: 99,579,042-100,932,403 , ACHE, 92 more genes
    nsv5926325copy number variation1nstd209human GRCh38 chr7: 100,126,046-100,145,306 , GRCh37.p13 chr7: 99,723,669-99,742,929 LAMTOR4, TAF6, 2 more genes
    nsv5867480copy number variation1nstd209human GRCh38 chr7: 100,126,595-100,134,180 , GRCh37.p13 chr7: 99,724,218-99,731,803 TAF6, MBLAC1
    nsv5853499copy number variation1nstd209human GRCh38 chr7: 100,121,106-100,134,130 , GRCh37.p13 chr7: 99,718,729-99,731,753 TAF6, CNPY4, 1 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5554296sequence alteration1nstd206human GRCh38 chr7: 100,117,686-100,117,708 , GRCh37.p13 chr7: 99,715,309-99,715,331 TAF6, CNPY4
    nsv5548483insertion1nstd206human GRCh38 chr7: 100,117,686-100,117,686 , GRCh37.p13 chr7: 99,715,309-99,715,309 CNPY4, TAF6
    nsv5381780copy number variation1nstd102humanPathogenic GRCh37 chr7: 87,477,185-100,333,327 , GRCh38.p12 chr7: 87,847,870-100,735,704 ARPC1A, LOC112267858, 265 more genes
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5259343copy number variation1nstd204human GRCh38.p13 chr7: 100,051,301-100,949,000 , GRCh37.p13 chr7: 99,648,924-100,546,632 , MEPCE, 70 more genes
    nsv5250151copy number variation1nstd204human GRCh37.p13 chr7: 99,719,424-99,755,923 , GRCh38.p13 chr7: 100,121,801-100,158,300 TAF6, TRAPPC14, 6 more genes
    nsv5112089mobile element insertion1nstd203human GRCh38 chr7: 100,121,894-100,121,909 , GRCh37.p13 chr7: 99,719,517-99,719,532 CNPY4, TAF6
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4966693copy number variation1nstd200human GRCh38 chr7: 100,117,346-100,117,502 , GRCh37.p13 chr7: 99,714,969-99,715,125 TAF6
    nsv4966692copy number variation1nstd200human GRCh38 chr7: 100,114,693-100,116,601 , GRCh37.p13 chr7: 99,712,316-99,714,224 TAF6
    nsv4966691copy number variation1nstd200human GRCh38 chr7: 100,108,804-100,109,067 , GRCh37.p13 chr7: 99,706,427-99,706,690 AP4M1, TAF6
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4819746copy number variation1nstd200human GRCh37 chr7: 99,714,069-99,714,667 , GRCh38.p12 chr7: 100,116,446-100,117,044 TAF6
    nsv4819745copy number variation1nstd200human GRCh37 chr7: 99,712,316-99,714,224 , GRCh38.p12 chr7: 100,114,693-100,116,601 TAF6
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